Variant report

Variant	rs10784563
Chromosome Location	chr12:67029900-67029901
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HELB-4	chr12:67029771-67029989	l_671_chr12:67024712-67029989_testes

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10784559	0.92[ASN][1000 genomes]
rs10784561	1.00[ASN][1000 genomes]
rs10784562	1.00[ASN][1000 genomes]
rs10784564	1.00[ASN][1000 genomes]
rs10784565	1.00[ASN][1000 genomes]
rs10784566	1.00[ASN][1000 genomes]
rs10784567	1.00[ASN][1000 genomes]
rs10784568	1.00[ASN][1000 genomes]
rs10878470	0.92[ASN][1000 genomes]
rs10878471	0.86[ASN][1000 genomes]
rs10878472	0.92[ASN][1000 genomes]
rs10878473	0.92[ASN][1000 genomes]
rs10878478	1.00[ASN][1000 genomes]
rs11176308	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs11176326	0.84[ASN][1000 genomes]
rs11176332	0.92[ASN][1000 genomes]
rs11176335	0.92[ASN][1000 genomes]
rs11176336	0.92[ASN][1000 genomes]
rs11176337	0.92[ASN][1000 genomes]
rs11176343	1.00[ASN][1000 genomes]
rs11176344	1.00[ASN][1000 genomes]
rs11176345	1.00[ASN][1000 genomes]
rs11176348	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11176349	1.00[ASN][1000 genomes]
rs11176350	1.00[ASN][1000 genomes]
rs11176351	1.00[ASN][1000 genomes]
rs11176352	1.00[ASN][1000 genomes]
rs11176354	1.00[ASN][1000 genomes]
rs11176355	1.00[ASN][1000 genomes]
rs11614834	0.84[ASN][1000 genomes]
rs12230590	0.92[ASN][1000 genomes]
rs12578666	0.84[ASN][1000 genomes]
rs12579975	0.84[ASN][1000 genomes]
rs34639740	0.89[ASN][1000 genomes]
rs4290313	1.00[ASN][1000 genomes]
rs4414309	1.00[ASN][1000 genomes]
rs4489824	1.00[ASN][1000 genomes]
rs4587801	1.00[ASN][1000 genomes]
rs55743225	0.81[ASN][1000 genomes]
rs57730465	1.00[ASN][1000 genomes]
rs61926094	0.92[ASN][1000 genomes]
rs61926104	1.00[ASN][1000 genomes]
rs73127190	1.00[ASN][1000 genomes]
rs7485667	1.00[ASN][1000 genomes]
rs7953437	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052503	chr12:66293898-67269495	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv541515	chr12:66293898-67269495	Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1040682	chr12:66750103-67328053	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv832449	chr12:66885819-67069953	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv469461	chr12:67007070-67038595	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv559208	chr12:67007070-67038595	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67023400-67033000	Weak transcription	Fetal Kidney	kidney
2	chr12:67025000-67030400	Weak transcription	Pancreas	Pancrea
3	chr12:67027800-67030000	Weak transcription	Colon Smooth Muscle	Colon
4	chr12:67028000-67030000	Weak transcription	Adipose Nuclei	Adipose
5	chr12:67028000-67030200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr12:67029200-67040000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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